chlorpromazine hydrochloride
Generic: chlorpromazine hydrochloride
Labeler: zydus lifesciences limitedDrug Facts
Product Profile
Brand Name
chlorpromazine hydrochloride
Generic Name
chlorpromazine hydrochloride
Labeler
zydus lifesciences limited
Dosage Form
INJECTION
Routes
Active Ingredients
chlorpromazine hydrochloride 25 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
70771-1779
Product ID
70771-1779_bdfa9437-bd3f-496f-a640-753422d69c85
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA217275
Listing Expiration
2026-12-31
Marketing Start
2024-03-29
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
707711779
Hyphenated Format
70771-1779
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
chlorpromazine hydrochloride (source: ndc)
Generic Name
chlorpromazine hydrochloride (source: ndc)
Application Number
ANDA217275 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/mL
Packaging
- 25 VIAL in 1 CARTON (70771-1779-7) / 2 mL in 1 VIAL (70771-1779-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "bdfa9437-bd3f-496f-a640-753422d69c85", "openfda": {"upc": ["0370710184971"], "unii": ["9WP59609J6"], "rxcui": ["1730076", "1730078"], "spl_set_id": ["d37a4c21-b503-4791-a4d0-2ccc8891d88e"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (70771-1779-7) / 2 mL in 1 VIAL (70771-1779-1)", "package_ndc": "70771-1779-7", "marketing_start_date": "20240329"}], "brand_name": "Chlorpromazine Hydrochloride", "product_id": "70771-1779_bdfa9437-bd3f-496f-a640-753422d69c85", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70771-1779", "generic_name": "Chlorpromazine Hydrochloride", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine Hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "25 mg/mL"}], "application_number": "ANDA217275", "marketing_category": "ANDA", "marketing_start_date": "20240329", "listing_expiration_date": "20261231"}